Trials / Completed
CompletedNCT05882760
Postoperative Sensitivity Following Placement with Different Restorative Materials in Vital Posterior Teeth
Comparison of Postoperative Sensitivity Following Placement with Different Restorative Materials in Vital Posterior Teeth
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 160 (actual)
- Sponsor
- Liaquat University of Medical & Health Sciences · Academic / Other
- Sex
- All
- Age
- 18 Years – 40 Years
- Healthy volunteers
- Accepted
Summary
There is a lack of long-term clinical studies comparing different restorative materials; most of the available studies have only looked at class I cavities or examined post-operative sensitivity in non-caries cervical lesions. The purpose of this study is to measure postoperative sensitivity in clinical settings at 3-month intervals for class 1 and 2 direct posterior restoration
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Tetric N Bond Universal® | Cavities will be restored with Conventional Hybrid Composite Restoration bonded with Etch \& Rinse Tetric - N - Bond (Ivoclar) |
| DRUG | Self Etch Tetric N Bond Universal® | Cavities will be restored with Conventional Hybrid Composite Restoration bonded with Self Etch Tetric N Bond Universal® |
| DRUG | GC Fuji IX, GC, Japan® | Cavities will be restored with GC Fuji IX, GC, Japan® |
| DRUG | Activa TM Bioactive Restorative ® | Cavities will be restored with Activa TM Bioactive Restorative ® |
Timeline
- Start date
- 2023-06-01
- Primary completion
- 2024-09-30
- Completion
- 2024-12-31
- First posted
- 2023-05-31
- Last updated
- 2025-03-06
Locations
1 site across 1 country: Pakistan
Source: ClinicalTrials.gov record NCT05882760. Inclusion in this directory is not an endorsement.